Basic information Safety Supplier Related

2'-TRIFLUOROMETHYL-BIPHENYL-4-CARBALDEHYDE

Basic information Safety Supplier Related

2'-TRIFLUOROMETHYL-BIPHENYL-4-CARBALDEHYDE Basic information

Product Name:
2'-TRIFLUOROMETHYL-BIPHENYL-4-CARBALDEHYDE
Synonyms:
  • 4-[2-(TRIFLUOROMETHYL)PHENYL]BENZALDEHYDE
  • AKOS BAR-1774
  • 2'-(TRIFLUOROMETHYL)[1,1'-BIPHENYL]-4-CARBALDEHYDE
  • [1,1'-Biphenyl]-4-carboxaldehyde, 2'-(trifluoromethyl)-
  • 2'-(Trifluoromethyl)[1,1'-biphenyl]-4-carboxaldehyde
  • 2'-(Trifluoromethyl)-[1,1'-biphenyl]-4-carbaldehyde
  • 2'-Trifluoromethyl-biphenyl-4-carbaldehyde
  • 2′-Trifluoromethyl-biphenyl-4-carbaldehyde, CAS 198205-95-7
CAS:
198205-95-7
MF:
C14H9F3O
MW:
250.22
Product Categories:
  • Biphenyl & Diphenyl ether
Mol File:
198205-95-7.mol
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2'-TRIFLUOROMETHYL-BIPHENYL-4-CARBALDEHYDE Chemical Properties

Boiling point:
338.8±42.0 °C(Predicted)
Density 
1.251±0.06 g/cm3(Predicted)
CAS DataBase Reference
198205-95-7(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36
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2'-TRIFLUOROMETHYL-BIPHENYL-4-CARBALDEHYDE Usage And Synthesis

Synthesis

392-83-6

87199-17-5

198205-95-7

A solution of tetrakis(triphenylphosphine)palladium (0.05 g) and sodium carbonate (0.7 g) in water (5 mL) was sequentially added to a stirred solution of o-bromobenzotrifluorotoluene (0.7 g, 2.75 mmol) and 4-formylbenzeneboronic acid (0.5 g, 3.3 mmol) in dioxane (20 mL) under nitrogen protection and at 80 °C. The reaction mixture was stirred at 100±5°C for 6 hours. Upon completion of the reaction, the solvent was removed by evaporation and the residue was diluted to 50 mL with ethyl acetate and washed with deionized water. The solvent was again removed by evaporation and the residue was purified by silica gel column chromatography (FCC) to afford 2'-(trifluoromethyl)-[1,1'-biphenyl]-4-carbaldehyde (0.61 g, 88% yield) as a milky white solid.1H-NMR (CDCl3) δ: 7.49 (d, 1H, J = 7.41 Hz); 7.48 (d, 2H, J = 8.13 Hz); 7.61-7.53 (m, 2H); 7.76 (d, 1H, J = 7.8 Hz); 7.91 (d, 2H, J = 8.34 Hz); 10.07 (s, 1H).

References

[1] Patent: WO2010/42998, 2010, A1. Location in patent: Page/Page column 95

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